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3 of 6,750 resources
Genome mapping and spliced alignment of cDNA or amino acid sequences
Tandem repeat genotyping with long reads, being a modified version of HipSTR.
This package provides a framework for the quantification and analysis of Short Reads. It covers a complete workflow starting from raw sequence reads, over creation of alignments and quality control plots, to the quantification of genomic regions of interest. Read alignments are either generated through Rbowtie (data from DNA/ChIP/ATAC/Bis-seq experiments) or Rhisat2 (data from RNA-seq experiments that require spliced alignments), or can be provided in the form of bam files.